A light-emitting composition containing first and second light-emitting markers. The first light-emitting marker comprises a first light-emitting material and a first binding group configured to bind to a first target analyte. The second light-emitting marker comprises a second light-emitting material which is different from the first light-emitting material and a second binding group which is different from the first binding group and which is configured to bind to a second target analyte. A luminescent lifetime of the first light-emitting material is shorter than a luminescent lifetime of the second light-emitting material. The difference in lifetimes of the first and second light-emitting materials may be used to distinguish between the first and second target analytes in a sample, e.g. by time-gated flow cytometry.
A method for manufacturing an LED lighting device includes forming a separation film on a substrate, patterning the separation film, forming LEDs on the separation film, bonding a stretch film to top surfaces of the LEDs and spacing between the LEDs, separating the separation film from the substrate, stretching the stretch film, exposing the top surfaces of the LEDs, and forming electrodes on the top surfaces of the LEDs, and a bottom surface of the separation film or bottom surfaces of the LEDs.
H01L 27/15 - Devices consisting of a plurality of semiconductor or other solid-state components formed in or on a common substrate including semiconductor components with at least one potential-jump barrier or surface barrier, specially adapted for light emission
This composition includes an olefin polymer A, an aliphatic polyester polymer B, and an inorganic powder C. The pH of the inorganic powder C evaluated per JIS M 8016-1991 is 6.5-11.5.
C08L 23/00 - Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
C08L 67/02 - Polyesters derived from dicarboxylic acids and dihydroxy compounds
C08K 3/013 - Fillers, pigments or reinforcing additives
4.
PELLETS, METHOD FOR PRODUCING PELLETS, AND METHOD FOR PRODUCING INJECTION-MOLDED ARTICLE
The present invention relates to pellets comprising a liquid crystal polyester resin, wherein an average length (L) of the pellets is 3.2 to 12 mm, an average diameter (D) of the pellets is 3.2 to 6.0 mm, and a value of the average length (L)/the average diameter (D) of the pellets is 1 to 2.
A composition comprising an electron-donating polymer and an electron acceptor wherein the electron-donating polymer comprises a benzo[1,2-b:4,5-b']dithiophene repeat unit and wherein a film of the electron-accepting material has a peak absorption wavelength greater than 1000 nm. The composition may be used as a photosensitive layer of an organic photodetector.
H10K 30/30 - Organic devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation comprising bulk heterojunctions, e.g. interpenetrating networks of donor and acceptor material domains
This method for producing a composition, which includes an olefin-based polymer A and a polyhydroxyalkanoate-based polymer B, and which contains 99.9-70 parts by mass of the olefin-based polymer A and 0.1-30 parts by mass of the polyhydroxyalkanoate-based polymer B with respect to the total 100 parts by mass of the olefin-based polymer A and the polyhydroxyalkanoate-based polymer B, comprises the steps of: supplying, to an extruder, a material 1 containing the olefin-based polymer A from a main feed port of the extruder and melting and kneading the material 1; and supplying, to the extruder, a material 2 containing the polyhydroxyalkanoate-based polymer B from a side feed port arranged on the downstream side of the main feed port in the extruder, and melting and kneading the material 2.
C08J 3/20 - Compounding polymers with additives, e.g. colouring
B29B 7/24 - Component parts, details or accessories; Auxiliary operations for feeding
C08K 3/013 - Fillers, pigments or reinforcing additives
C08L 23/00 - Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
C08L 67/04 - Polyesters derived from hydroxy carboxylic acids, e.g. lactones
7.
SULFONAMIDE COMPOUND AND HARMFUL-ARTHROPOD CONTROLLING COMPOSITION CONTAINING SAME
The present invention provides a compound having an excellent control effect against harmful arthropods. A compound represented by formula (1) and an N oxide thereof have an excellent control effect against harmful arthropods. [In the formula, Q shown in the formula below (where # represents a site of bonding with a sulfur atom and ● represents a site of bonding with Het) is, for example, a group represented by formula Q1; R2aand R2bare the same or different from each other and represent, for example, a C1-C6 alkyl group that may be substituted with one or more halogen atoms; R3a, R3b, and R3dare the same or different from each other and represent, for example, a hydrogen atom; Het represents, for example, a group represented by formula Het1; A2represents a nitrogen atom or CR4a; W1represents an oxygen atom or a sulfur atom; R4arepresents, for example, a C1-C6 chain hydrocarbon group; the combination of B1, B2, B3, and B4represents, for example, a combination in which B1is a nitrogen atom or CR6a, B2is CR6e, B3is a nitrogen atom or CR6c, and B4is a nitrogen atom or CR6d; R6a, R6c, and R6dare the same or different from each other and represent, for example, a hydrogen atom; and R6e represents, for example, a C1-C6 chain hydrocarbon group that is substituted with one or more substituents selected from the group consisting of cyano groups and a halogen atom.]
A01N 43/90 - Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having two or more relevant hetero rings, condensed among themselves or with a common carbocyclic ring system
A61K 31/437 - Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
A61K 31/444 - Non-condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring hetero atom, e.g. amrinone
C07D 519/00 - Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups or
8.
SULFONAMIDE COMPOUND AND HARMFUL-ARTHROPOD-CONTROLLING COMPOSITION CONTAINING SAME
The present invention provides a compound, or an N-oxide thereof, which has an excellent controlling effect with respect to harmful arthropods and which is represented by formula (I) (in the formula: Q denotes a group represented by formula Q1, or the like; R2aand R2b, which may be the same or different, denote a C1-C6 alkyl group that may be substituted with one or more halogen atoms, or the like; and Het denotes a group represented by formula Het1, or the like).
A01M 1/20 - Poisoning, narcotising, or burning insects
A01N 43/40 - Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings
A01N 43/90 - Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having two or more relevant hetero rings, condensed among themselves or with a common carbocyclic ring system
A01N 47/02 - Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having no bond to a nitrogen atom
The present invention provides a compound represented by formula (I) [wherein, Q represented by the formula below (wherein # represents a binding site with a sulfur atom, and ● represents a binding site with Het) represents, inter alia, a group represented by formula Q1; R2aand R2bare identical with each other or different from each other and represent, inter alia, a C1-C6 alkyl group that may be substituted by one or more halogen atoms; R3a, R3b, and R3dare identical with each other or different from each other and represent, inter alai, a hydrogen atom; Het represents, inter alia, a group represented by the formula Het5; A2represents NR5aor CR4aR4d; A3represents CR4bR4e; W1represents an oxygen atom or a sulfur atom; when Het is a group represented by formula Het5, the combination of B1, B2, and B3represents, inter alia, a combination in which B1is CR6e, B2is a nitrogen atom or CR6b, and B3is a nitrogen atom or CR6c; R4a, R4b, R6a, R6b, and R6care identical with each other or different from each other and represent, inter alia, a hydrogen atom; R4dand R4eare identical with each other or different from each other and represent a hydrogen atom, etc.; R6erepresents, inter alia, a C1-C6 chain hydrocarbon group that has been substituted by one or more substituents selected from the group consisting of cyano groups and halogen atoms; and R5a represents a hydrogen atom, etc.] or an N-oxide thereof, said compound having an an excellent control effect against harmful arthropods.
C07D 401/04 - Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring- member bond
A01M 1/20 - Poisoning, narcotising, or burning insects
A01N 43/42 - Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings condensed with carbocyclic rings
A01N 43/90 - Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having two or more relevant hetero rings, condensed among themselves or with a common carbocyclic ring system
A01N 47/02 - Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having no bond to a nitrogen atom
A01N 53/12 - Compounds containing the group , X or Y being a nitrogen atom, e.g. cyclopropane carboxylic acid amides
A method of treating a reaction mixture comprising light-emitting nanoparticles formed upon reaction of a silica-forming compound in the presence of a light-emitting material in a protic, water-miscible solvent. The method comprises forming a phase-separated system comprising: an aqueous phase comprising the protic, water miscible solvent, an organic phase comprising an organic solvent and a separating solvent; and separating the organic phase. The separating solvent is immiscible with water, miscible with the water-miscible protic solvent and miscible with the organic solvent.
The present invention addresses the problem of providing a polymer that suppresses dark current in a photoelectric conversion element. The present invention pertains to a polymer that has structural unit having a main chain and a side chain. The weighted average of the formula weight of the side chain weighted with the mole fraction of the structural unit included in the polymer is 160 or more. The absorption edge intensity of the polymer is 0.08 or less.
C08G 85/00 - General processes for preparing compounds provided for in this subclass
C08G 61/12 - Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule
C08L 65/00 - Compositions of macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain; Compositions of derivatives of such polymers
C08L 101/12 - Compositions of unspecified macromolecular compounds characterised by physical features, e.g. anisotropy, viscosity or electrical conductivity
C09D 11/102 - Printing inks based on artificial resins containing macromolecular compounds obtained by reactions other than those only involving unsaturated carbon-to-carbon bonds
C09D 165/00 - Coating compositions based on macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain; Coating compositions based on derivatives of such polymers
H10K 30/60 - Organic devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation in which radiation controls flow of current through the devices, e.g. photoresistors
H10K 39/00 - Integrated devices, or assemblies of multiple devices, comprising at least one organic radiation-sensitive element covered by group
12.
LITHIUM-METAL COMPLEX OXIDE, POSITIVE ELECTRODE ACTIVE MATERIAL FOR LITHIUM SECONDARY BATTERY, POSITIVE ELECTRODE FOR LITHIUM SECONDARY BATTERY, AND LITHIUM SECONDARY BATTERY
This lithium-metal complex oxide includes at least Li and Ni, and satisfies (1) and (2). (1) In a pore size distribution in the adsorption isotherm as determined using adsorption isotherm and desorption isotherm measurements of nitrogen gas and the Barrett-Joyner-Halenda method, the pore volume in the range in which the pore diameter is 2 to 10 nm is greater than 0.4×10–3cm3/g and less than or equal to 1.0×10–3cm35050 is 0.9×10–3to 3.4×10–3.
H01M 4/505 - Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of manganese of mixed oxides or hydroxides containing manganese for inserting or intercalating light metals, e.g. LiMn2O4 or LiMn2OxFy
H01M 4/525 - Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of nickel, cobalt or iron of mixed oxides or hydroxides containing iron, cobalt or nickel for inserting or intercalating light metals, e.g. LiNiO2, LiCoO2 or LiCoOxFy
13.
STABILIZER, ORGANIC MATERIAL COMPOSITION, AND ORGANIC MATERIAL STABILIZING METHOD
The present invention pertains to a stabilizer which comprises: a compound (A) selected from the group consisting of compounds represented by formula (1) [in formula (1), R1, R2, R4, and R5each independently represent a hydrogen atom, an alkyl group having 1-8 carbon atoms, a cycloalkyl group having 5-8 carbon atoms, an alkyl cycloalkyl group having 6-12 carbon atoms, an aralkyl group having 7-12 carbon atoms, or a phenyl group, each R3independently represents a hydrogen atom or an alkyl group having 1-8 carbon atoms, X represents a single bond, a sulfur atom, or a -CH(-R13)-group (R13represents a hydrogen atom, an alkyl group having 1-8 carbon atoms, or a cycloalkyl group having 5-8 carbon atoms), A represents an alkylene group having 1-8 carbon atoms or a *-C(=O)-R14-group (R14represents a single bond or an alkylene group having 1-8 carbon atoms, and * represents an atomic bonding on the oxygen side), and one of Y and Z represents a hydroxyl group, an alkoxy group having 1-8 carbon atoms, or an aralkyloxy group having 7-12 carbon atoms, and the other of Y and Z represents a hydrogen atom or an alkyl group having 1-8 carbon atoms] and compounds represented by formula (2) [in formula (2), R6and R8each independently represent a hydrogen atom, a methyl group, or an alkyl group having 5-8 carbon atoms, each R7independently represents a hydrogen atom or a hydroxyl group, and each R91525-3125-31 group, but at least one of R6, R7, R8, or R9is not a hydrogen atom]; and a compound (B) represented by formula (3) [in formula (3), R10, R11, and R12each independently represent a hydrogen atom, an alkyl group having 1-12 carbon atoms, or an arylalkyl group having a total of 7-20 carbon atoms, but at least one of R10, R11, and R12 is not a hydrogen atom]. In the stabilizer, the contained amount of the compound (B) with respect to 100 parts by mass of the compound (A) is 0.01-50 parts by mass.
The purpose of the present invention is to provide a pest control agent in which Bacillus bacteria are diluted in advance with water to a prescribed concentration range (especially a spray concentration range), the pest control agent having improved storage stability. The present invention provides a pH-adjusted stabilized pest control agent that contains Bacillus bacteria, a pH adjuster, and water.
Disclosed is a color filter comprising a glass substrate, a frit formed on the glass substrate, a pattern boundary unit formed inside the frit on the glass substrate, black matrix (BM) layers formed inside the pattern boundary unit on the glass substrate, a first colored layer formed between the BM layers, and a second colored layer formed between the pattern boundary unit and the BM layers.
G03F 7/00 - Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printed surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
A feed for livestock is provided that shows excellent weight gain and improved feed efficiency. A feed additive composition and a feed for livestock comprising abscisic acid and/or a salt thereof and glutamic acid; a method of feeding livestock, a method of improving the weight gain of livestock, and a method of increasing the feed efficiency in livestock, comprising letting livestock to take said feed; and a use of the feed for livestock for improving the weight gain of livestock, and a use of the feed for increasing the feed efficiency in livestock.
The present invention provides a method for controlling a soybean rust fungus having an amino acid substitution of F129L on mitochondrial cytochrome b protein, by applying a compound represented by formula (I) [wherein Q represents a group represented by the following Q1, Q2, Q3, Q4 or Q5 (in the formulae, • represents a binding site to benzene ring); X represents an oxygen atom or NH; L represents CH2, an oxygen atom or NCH3; E represents a C6-C10 aryl group, etc.; R1 represents a C1-C3 chain hydrocarbon group or a cyclopropyl group, etc.; R2 represents a C1-C3 chain hydrocarbon group or a cyclopropyl group, etc.; R3 represents a C1-C3 alkoxy group or a C1-C3 chain hydrocarbon group, etc.; and n is 0, 1, 2, or 3] or its N oxide or an agriculturally acceptable salt thereof.
The present invention provides a method for controlling a soybean rust fungus having an amino acid substitution of F129L on mitochondrial cytochrome b protein, by applying a compound represented by formula (I) [wherein Q represents a group represented by the following Q1, Q2, Q3, Q4 or Q5 (in the formulae, • represents a binding site to benzene ring); X represents an oxygen atom or NH; L represents CH2, an oxygen atom or NCH3; E represents a C6-C10 aryl group, etc.; R1 represents a C1-C3 chain hydrocarbon group or a cyclopropyl group, etc.; R2 represents a C1-C3 chain hydrocarbon group or a cyclopropyl group, etc.; R3 represents a C1-C3 alkoxy group or a C1-C3 chain hydrocarbon group, etc.; and n is 0, 1, 2, or 3] or its N oxide or an agriculturally acceptable salt thereof.
A01N 37/12 - Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group , wherein Cn means a carbon skeleton not containing a ring; Thio-analogues thereof
The present invention provides an efficient process for preparing a nucleic acid oligomer, in particular, a process for deprotecting efficiently a protecting group of hydroxy group of a ribose in a nucleic acid oligomer. Specifically, the present invention also provides a process for preparing a nucleic acid oligomer represented by formula (4), which comprises contacting a nucleic acid oligomer represented by formula (3) with a fluoride ion under an atmosphere of an inert gas or inert gases containing 15% or less of oxygen concentration (wherein the definitions of each groups described in formula (3) and formula (4) are the same as defined in the Description).
The present invention provides an efficient process for preparing a nucleic acid oligomer, in particular, a process for deprotecting efficiently a protecting group of hydroxy group of a ribose in a nucleic acid oligomer. Specifically, the present invention also provides a process for preparing a nucleic acid oligomer represented by formula (4), which comprises contacting a nucleic acid oligomer represented by formula (3) with a fluoride ion under an atmosphere of an inert gas or inert gases containing 15% or less of oxygen concentration (wherein the definitions of each groups described in formula (3) and formula (4) are the same as defined in the Description).
C07H 21/00 - Compounds containing two or more mononucleotide units having separate phosphate or polyphosphate groups linked by saccharide radicals of nucleoside groups, e.g. nucleic acids
19.
REACTIVE COMPOUND, PRODUCTION METHOD FOR POLYMER COMPOUND, AND INTERMEDIATE
(Abstract) (Problem) To provide a (meth)acrylic resin composition which exhibits excellent heat resistance, a film formed from the same and a polarizing plate containing said film. (Solution) Provided are: a (meth)acrylic resin composition which contains a (meth)acrylic resin (A), an elastomer component (B) and an oxidation inhibitor (C), wherein the mass ratio of the content of the oxidation inhibitor (C) to the content of the elastomer component (B) is 0.006-0.2, inclusive; a film formed from the same; and a polarizing plate containing said film. [Selected drawing] None
Disclosed is a composition including a compound of formula (1), a compound of formula (2) having a maximum absorption wavelength of 550 nm or more and 650 nm or less, and a liquid crystalline compound. n and m are 1 or 2. R1 and R3 represent a substituent. R2 and R4 represent an alkylamino group, an alkoxy group, or an alkylthio group. P represents a single bond, —OC(═O)—, —C(═O)O—, —NHC(═O)—, —C(═O)NH—, —C≡C—, —CH═CH—, —CH═N—, —N═N—, and —N═CH—. Ar1, Ar2, and Ar3 represent a 1,4-phenylene group or a divalent sulfur-containing aromatic heterocyclic group, and at least one of Ar1 and Ar2 is substituted with fluorine. Ar4, Ar5, and Ar6 represent a 1,4-phenylene group, a naphthalenediyl group, or a divalent sulfur-containing aromatic heterocyclic group.
Disclosed is a composition including a compound of formula (1), a compound of formula (2) having a maximum absorption wavelength of 550 nm or more and 650 nm or less, and a liquid crystalline compound. n and m are 1 or 2. R1 and R3 represent a substituent. R2 and R4 represent an alkylamino group, an alkoxy group, or an alkylthio group. P represents a single bond, —OC(═O)—, —C(═O)O—, —NHC(═O)—, —C(═O)NH—, —C≡C—, —CH═CH—, —CH═N—, —N═N—, and —N═CH—. Ar1, Ar2, and Ar3 represent a 1,4-phenylene group or a divalent sulfur-containing aromatic heterocyclic group, and at least one of Ar1 and Ar2 is substituted with fluorine. Ar4, Ar5, and Ar6 represent a 1,4-phenylene group, a naphthalenediyl group, or a divalent sulfur-containing aromatic heterocyclic group.
H10K 85/40 - Organosilicon compounds, e.g. TIPS pentacene
C09K 19/20 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings linked by a chain containing carbon and oxygen atoms as chain links, e.g. esters
C09K 19/30 - Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing saturated or unsaturated non-aromatic rings, e.g. cyclohexane rings
H10K 85/60 - Organic compounds having low molecular weight
22.
POLARIZING PLATE FOR ANTIREFLECTION AND DISPLAY DEVICE COMPRISING THE SAME
Provided are a polarizing plate for antireflection including a polarizer, and a protective layer formed on at least one surface of the polarizer, wherein the polarizing plate has a single transmittance of 44.6% or more and a degree of polarization of 98% or more and satisfies 0≤[(orthogonal a*)2+(orthogonal b*)2]0.5≤16, and a display device including the polarizing plate. The polarizing plate for antireflection can exhibit high transmittance while preventing blue-shift phenomenon and having neutral reflection color. Further, the polarizing plate for antireflection can be made thinner.
The present invention addresses the problem of providing a composition capable of forming an optical filter that has fewer aggregates. The present invention relates to a composition comprising a near-infrared absorbing dye, an alkali-soluble resin, and a solvent, wherein the near-infrared absorbing dye comprises a compound represented by formula (I). (In formula (I), R1, R4, R5, and R8each independently represent a C1-20 hydrocarbon group or the like; R2, R3, R6, and R7each independently represent a hydrogen atom or the like; R9, R10, and R11each independently represent a C1-20 hydrocarbon group, and if two or more R11moieties are present, said moieties may be the same or different; X1-X4each independently represent a hydrogen atom or the like; Y1-Y8each independently represent a hydrogen atom or the like; and R12represents a C1-5 alkyl group, and if two or more R12 moieties are present, said moieties may be the same or different)
(Abstract) (Problem) To provide an optical laminate in which a release film can be satisfactorily released from an adhesive layer. (Solution) This optical laminate includes an optical film, an adhesive layer, and a release film in the stated order. The release film has a release treatment surface containing a siloxane compound on a side where the release film makes contact with the adhesive layer. The release treatment surface of the release film satisfies the relationship indicated by formula (1). (1): Ys/Xs × 100 ≤ 3.5 [In formula (1), Xs represents the intensity of the maximum peak Ps in a binding energy range of 96-108 eV of an XPS spectrum (Sr) of the release treatment surface, and Ys represents the intensity of the XPS spectrum (Sr) at a binding energy of (Es + 2) eV, when the binding energy at the peak PS is Es [eV].] (Selected figure) FIG. 1
The present invention provides a compound having excellent control efficacy against plant diseases. A compound represented by formula (I) has excellent control efficacy against plant diseases.
C07C 69/74 - Esters of carboxylic acids having an esterified carboxyl group bound to a carbon atom of a ring other than a six-membered aromatic ring
A01N 53/06 - Esters containing the group , wherein the carbon atom marked with an asterisk is acyclic or part of a ring or ring system; Thio-analogues thereof the carbon atom marked with an asterisk being acyclic and directly bound to a carbon atom of a six-membered aromatic ring, e.g. benzyl esters; Thio-analogues thereof
The present invention addresses the problem of preventing the blockage of pipes and preventing combustion and explosion. The present invention relates to a regeneration system 1 that is for regenerating methyl (meth)acrylate from scraps of molded bodies obtained by molding a (meth)acrylic resin composition containing a (meth)acrylic polymer and comprises: a pyrolysis device 10 that has a loading section 12 and a gas removal section 14; a first capture tank 52 that has gas containing methyl (meth)acrylate introduced thereinto and serves to capture a residue containing undecomposed components included in the gas containing methyl (meth)acrylate and remove the residue containing undecomposed components; and a gas processing device 70 selected from the group consisting of a purifier for purifying gas containing methyl (meth)acrylate processed by the first capture tank and a cooler for cooling gas containing methyl (meth)acrylate.
C08J 11/12 - Recovery or working-up of waste materials of polymers by chemically breaking down the molecular chains of polymers or breaking of crosslinks, e.g. devulcanisation by dry-heat treatment only
C07C 67/475 - Preparation of carboxylic acid esters by splitting of carbon-to-carbon bonds and redistribution, e.g. disproportionation or migration of groups between different molecules
Provided is an inorganic fine particle dispersion capable of forming a layer having even higher light transmittance and exceptional antifouling properties. This inorganic fine particle dispersion contains inorganic fine particles, a liquid dispersion medium A having a boiling point higher than 121°C but lower than 190°C, a liquid dispersion medium B having a boiling point lower than 100°C, water, an alkoxysilane, and a pore-forming agent, wherein the percentage content of the liquid dispersion medium A is at least 0.5 mass% but less than 15.0 mass% per 100 mass% of the total amount of the inorganic fine particle dispersion.
C09D 17/00 - Pigment pastes, e.g. for mixing in paints
B05D 7/24 - Processes, other than flocking, specially adapted for applying liquids or other fluent materials to particular surfaces or for applying particular liquids or other fluent materials for applying particular liquids or other fluent materials
B32B 5/22 - Layered products characterised by the non-homogeneity or physical structure of a layer characterised by the presence of two or more layers which comprise fibres, filaments, granules, or powder, or are foamed or specifically porous
C09D 1/00 - Coating compositions, e.g. paints, varnishes or lacquers, based on inorganic substances
According to the present invention, a compound represented by formula (I) (wherein, Q (# denotes a bonding site with a sulfur atom, and ● denotes a bonding site with Het) represented in the formula denotes a group or the like represented by formula Q1, R2aand R2bmay be the same or different and represent a C1-C6 alkyl group or the like that may be substituted with one or more halogen atoms, R3a, R3b, and R3dmay be the same or different and represent a hydrogen atom or the like, Het represents a group or the like represented by formula Het1, A2represents a nitrogen atom or CR4a, A3represents a nitrogen atom or CR4b, W1represents an oxygen atom or a sulfur atom, R4aand R4bmay be the same or different and represent a C1-C6 chain hydrocarbon group or the like, R6 represents a C1-C6 chain hydrocarbon group or the like, and T represents a C1-C10 chain hydrocarbon group {the C1-C10 chain hydrocarbon group having one or more substituents selected from the group consisting of a cyano group and a halogen atom} or the like) exhibits an excellent extermination effect against harmful arthropods.
A01N 43/40 - Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings
A01N 43/90 - Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having two or more relevant hetero rings, condensed among themselves or with a common carbocyclic ring system
A61K 31/444 - Non-condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring hetero atom, e.g. amrinone
A61K 31/506 - Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
A61K 31/517 - Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with carbocyclic ring systems, e.g. quinazoline, perimidine
C07D 401/04 - Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring- member bond
C07D 519/00 - Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups or
29.
CYCLOPROPANECARBOXYLIC ACID ESTER COMPOUND AND USE THEREOF
The present invention provides a compound having excellent control efficacy against plant diseases. The compound, represented by formula (I), has excellent control efficacy against plant diseases.
C07D 303/40 - Compounds containing oxirane rings with hydrocarbon radicals, substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals by ester radicals
A01N 53/06 - Esters containing the group , wherein the carbon atom marked with an asterisk is acyclic or part of a ring or ring system; Thio-analogues thereof the carbon atom marked with an asterisk being acyclic and directly bound to a carbon atom of a six-membered aromatic ring, e.g. benzyl esters; Thio-analogues thereof
A01P 1/00 - Disinfectants; Antimicrobial compounds or mixtures thereof
The present invention provides a compound having excellent control efficacy against plant diseases. The compound, represented by formula (I), has excellent control efficacy against plant diseases (in the formula, R represents a 2-hydroxypropan-2-yl group or a 1-propen-2-yl group).
31.
CYCLOPROPANECARBOXYLIC ACID ESTER COMPOUND AND USE THEREOF
The present invention provides a compound having excellent control efficacy against plant diseases. The compound, represented by formula (I), has excellent control efficacy against plant diseases (in the formula, R represents a chlorine atom or a hydroxy group).
The present invention provides a compound having excellent control efficacy against plant diseases. The compound, represented by formula (I), has excellent control efficacy against plant diseases (in the formula, R represents a 1-propen-2-yl group or a 2-hydroxypropan-2-yl group).
The present invention provides a compound having excellent control efficacy against plant diseases. The compound, represented by formula (I), has excellent control efficacy against plant diseases (in the formula, R represents a vinyl group or a 1-hydroxyethyl group).
The present invention provides a compound having excellent control efficacy against plant diseases. The compound, represented by formula (I), has excellent control efficacy against plant diseases (in the formula, R represents a 2-hydroxypropan-2-yl group or a 1-propen-2-yl group).
The present invention provides a compound having excellent control efficacy against plant diseases. The compound, represented by formula (I), has excellent control efficacy against plant diseases (in the formula, for R1and R2, R1represents a hydrogen atom and R2represents a 1-propen-2-yl group, or R1and R2 are united and represent an isopropylidene group).
The present invention relates to an infrared ray-transmitting photosensitive resin composition comprising a colorant, an alkali-soluble resin, a photopolymerizable compound, a photopolymerization initiator, and a solvent, wherein the infrared ray-transmitting photosensitive resin composition comprises at least one of a porphyrin compound and a chromatic colorant of a specific color. The infrared ray-transmitting photosensitive resin composition, according to the present invention, exhibits a high transmittance in the infrared region and a low transmittance in the visible light region, even in a thin film, and has excellent patterning properties.
G03F 7/031 - Organic compounds not covered by group
G03F 7/105 - Photosensitive materials - characterised by structural details, e.g. supports, auxiliary layers having substances, e.g. indicators, for forming visible images
G03F 7/00 - Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printed surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
C08L 101/00 - Compositions of unspecified macromolecular compounds
Provided is a pesticidal composition comprising a compound represented by the formula (I), a herbicidal active salt, an organic solvent having a water solubility at 25° C. of 10 mass % or less, a surfactant and water, wherein a weight ratio between the compound represented by the formula (I) and the surfactant is 1:10 or more and 1:50 or less.
Provided is a pesticidal composition comprising a compound represented by the formula (I), a herbicidal active salt, an organic solvent having a water solubility at 25° C. of 10 mass % or less, a surfactant and water, wherein a weight ratio between the compound represented by the formula (I) and the surfactant is 1:10 or more and 1:50 or less.
A01N 37/40 - Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio-analogue, or a derivative thereof, and a singly bound oxygen or sulfur atom attached to the same carbon skeleton, this oxygen or sulfur atom not being a member of a carboxylic group or of a thio-anal having at least one oxygen or sulfur atom attached to an aromatic ring system having at least one carboxylic group or a thio-analogue, or a derivative thereof, and one oxygen or sulfur atom attached to the same aromatic ring system
LIQUID CRYSTAL POLYESTER POWDER, METHOD FOR PRODUCING POWDER, COMPOSITION, METHOD FOR PRODUCING COMPOSITION, METHOD FOR PRODUCING FILM, AND METHOD FOR PRODUCING LAMINATED BODY
The present invention relates to a liquid crystal polyester powder comprising a liquid crystal polyester, wherein the liquid crystal polyester has a flow starting temperature of 255° C. or less and has a structural unit comprising a naphthalene structure, and, when a particle diameter at which a cumulative volume proportion from a small particle side in a volume-based cumulative particle diameter distribution curve by laser diffraction/scattering type particle diameter distribution measurement is 50% is defined as D50, D50 is 0.1 to 30 μm.
C08L 67/00 - Compositions of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Compositions of derivatives of such polymers
Provided is a method for producing elastomer pellets, the method comprising a step for hot-cutting an elastomer, in which the step for hot-cutting the elastomer includes cooling the elastomer extruded through the die hole with cooling water, and the value of a parameter A represented by general formula (I) is 1.8 or less. (I): A=-X0.41-Y0.36+Z0.71 (In general formula (I), X represents the weight average molecular weight (unit: ten-thousand) of the elastomer; Y represents the shear rate [1/sec] of the elastomer in the die hole; and Z represents the temperature [°C] of the cooling water for the elastomer.)
B29B 9/06 - Making granules by dividing preformed material in the form of filamentary material, e.g. combined with extrusion
C08F 236/10 - Copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds the radical having only two carbon-to-carbon double bonds conjugated with vinyl aromatic monomers
40.
METHYL (METH)ACRYLATE RECYCLING SYSTEM, AND METHOD FOR RECYCLING METHYL (METH)ACRYLATE
The present invention addresses the problem of preventing the opening and closing of distribution channels and further preventing ignition and explosion. The present invention pertains to a recycling system comprising: a pyrolysis device 10 for pyrolyzing scrap to produce gas containing methyl (meth)acrylate and a residue containing undecomposed components; and a residue storage device 30 for storing the residue containing undecomposed components derived from the pyrolysis device, wherein the pyrolysis device has an input section 12, a gas extraction section 14 for extracting gas generated by the pyrolysis of a (meth)acrylic resin composition, and a residue discharge section 16 for discharging the residue containing undecomposed components to the residue storage device, and the residue storage device has a storage tank 32.
C08J 11/12 - Recovery or working-up of waste materials of polymers by chemically breaking down the molecular chains of polymers or breaking of crosslinks, e.g. devulcanisation by dry-heat treatment only
B29B 17/00 - Recovery of plastics or other constituents of waste material containing plastics
41.
SYSTEM FOR REGENERATING METHYL (METH)ACRYLATE AND METHOD FOR REGENERATING METHYL (METH)ACRYLATE
The present invention prevents ignition and explosion in a connecting pipe. A regeneration system 1 in the present invention comprises: a thermal decomposition apparatus 10 for thermally decomposing scraps of molded bodies obtained by molding a (meth)acrylic resin composition containing a (meth)acrylic polymer, the thermal decomposition apparatus comprising an introduction unit 12 for introducing scraps, and a gas discharge unit 14 for discharging a methyl (meth)acrylate-containing gas generated by the thermal decomposition of the (meth)acrylic resin composition; and a gas treatment apparatus 30 which is connected to the gas discharge unit 14 via a connecting pipe 20 and which includes at least one type selected from the group consisting of a refining unit for refining a gas discharged via the connecting pipe and a cooling unit for cooling the gas. The connecting pipe includes at least one pipe main body 22A, and at least a partial region of the pipe main body has a cooling unit 24 for cooling a gas that passes through the pipe main body.
C08J 11/12 - Recovery or working-up of waste materials of polymers by chemically breaking down the molecular chains of polymers or breaking of crosslinks, e.g. devulcanisation by dry-heat treatment only
C07C 67/475 - Preparation of carboxylic acid esters by splitting of carbon-to-carbon bonds and redistribution, e.g. disproportionation or migration of groups between different molecules
The present invention provides a compound having an excellent control effect on harmful arthropods. A compound represented by formula (I) [wherein the meaning of each symbol is as described in the description] or N-oxide thereof has an excellent control effect on harmful arthropods.
A01N 43/90 - Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having two or more relevant hetero rings, condensed among themselves or with a common carbocyclic ring system
A61K 31/437 - Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
The present invention provides an excellent control method against plant diseases. A compound represented by formula (I) or an N oxide thereof or salts thereof can be used for controlling plant diseases (in the formula, Z represents a C6-C10 aryl group, etc.; R1and R2are the same as or different from each other and each represents a C1-C6 chain hydrocarbon group, etc.; R3represents a C1-C6 chain hydrocarbon group or the like; adjacent R1and R3may be combined with a carbon atom to which they are bonded to form a C4-C7 alicyclic hydrocarbon; adjacent two R3and R3may be combined with a carbon atom to which they are bonded, to thereby form a C4-C7 alicyclic hydrocarbon; and p represents 0, 1, 2, or 3, and, when p is 2 or 3, two or three R3s may be the same as or different from each other.).
C07D 401/12 - Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
44.
CYCLOPROPANECARBOXYLIC ACID ESTER COMPOUND AND USE THEREOF
The present invention provides a compound having excellent control efficacy against plant diseases. The compound, represented by formula (I), has excellent control efficacy against plant diseases.
C07C 69/757 - Esters of carboxylic acids having an esterified carboxyl group bound to a carbon atom of a ring other than a six-membered aromatic ring having any of the groups OH, O-metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety
A01N 53/06 - Esters containing the group , wherein the carbon atom marked with an asterisk is acyclic or part of a ring or ring system; Thio-analogues thereof the carbon atom marked with an asterisk being acyclic and directly bound to a carbon atom of a six-membered aromatic ring, e.g. benzyl esters; Thio-analogues thereof
A01P 1/00 - Disinfectants; Antimicrobial compounds or mixtures thereof
The present invention provides a compound having excellent control efficacy against harmful arthropods. The compound, represented by formula (I), has excellent control efficacy against harmful arthropods.
The present invention provides a compound having excellent control efficacy against plant diseases. The compound, represented by formula 1, has excellent control efficacy against plant diseases (in the formula, for R1and R2, R1represents a hydrogen atom and R2represents a 1-propen-2-yl group or a 2-hydroxypropan-2-yl group, or R1and R2 are united and represent an isopropylidene group).
The present invention provides a method for producing elastomer pellets, the method comprising a step for hot cutting an elastomer that is extruded from a die hole of a die, wherein the value of parameter A that is expressed by general formula (I) is 3.5 or more. (I): A = 0.066 × X + 0.135 × Y (In general formula (I), X represents the shear rate (1/sec) of the elastomer in the die hole; Y represents the stress relaxation torque integral value (dNm∙sec) of the elastomer; and the stress relaxation torque integral value is obtained by integrating the torque values from 0.01 second to 10 seconds with respect to the torque curve that is obtained from a double logarithmic plot of stress relaxation times and torques, which are measured by performing a stress relaxation test of the elastomer at the temperature of 50°C and the strain rate of 13.95%.)
B29B 9/06 - Making granules by dividing preformed material in the form of filamentary material, e.g. combined with extrusion
C08F 236/10 - Copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds the radical having only two carbon-to-carbon double bonds conjugated with vinyl aromatic monomers
48.
LIQUID-CRYSTAL POLYESTER COMPOSITION, METHOD FOR PRODUCING LIQUID-CRYSTAL POLYESTER COMPOSITION, AND MOLDED OBJECT
The present invention relates to a liquid-crystal polyester composition which comprises a liquid-crystal polyester and an olefin copolymer, wherein the olefin copolymer comprises repeating unit A derived from a C2-C8 olefin monomer and repeating unit B having a glycidyl group.
C08L 67/00 - Compositions of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Compositions of derivatives of such polymers
C08F 210/00 - Copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
C08G 63/02 - Polyesters derived from hydroxy carboxylic acids or from polycarboxylic acids and polyhydroxy compounds
C08G 63/06 - Polyesters derived from hydroxy carboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from hydroxy carboxylic acids
C08L 23/02 - Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
C08L 63/10 - Epoxy resins modified by unsaturated compounds
49.
HARD COATING FILM AND IMAGE DISPLAY DEVICE HAVING SAME
ITITIT) is controlled to a specific range, so that high hardness, excellent scratch resistance, and excellent bending resistance are exhibited, enabling repeated folding.
C09D 133/06 - Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, the oxygen atom being present only as part of the carboxyl radical
G06F 3/041 - Digitisers, e.g. for touch screens or touch pads, characterised by the transducing means
G09F 9/30 - Indicating arrangements for variable information in which the information is built-up on a support by selection or combination of individual elements in which the desired character or characters are formed by combining individual elements
The present invention relates to a liquid crystal polyester powder comprising a liquid crystal polyester, wherein, when a particle diameter at which a cumulative volume proportion from a small particle side in a volume-based cumulative particle diameter distribution curve by laser diffraction/scattering type particle diameter distribution measurement is 90% is defined as D90, D90 is 20 μm or less.
A method for producing a phosphor having a core-shell structure that includes: a core part formed of a crystal phase of an inorganic compound containing a metal element M constituting a luminescent center ion and aluminum; and a shell part containing at least one element selected from the group consisting of boron and silicon and formed on at least a portion of a surface of the core part, the method including: mixing a raw material of the crystal phase and a raw material of the shell part; and heating the obtained mixture at a temperature at which the raw material of the shell part is liquefied, but a host crystal of a phosphor to be obtained is maintained, in which the raw material of the crystal phase contains a raw material compound having D50 in a particle diameter distribution of 0.2 to 90 μm and containing aluminum.
The present invention pertains to, inter alia, a resin composition containing a liquid crystal polyester and a thermoplastic polyimide. The liquid crystal polyester has a repeating unit containing a naphthalene structure, and the number of the repeating units containing the naphthalene structure is 60% or more in relation to a total of 100% of all repeating units in the liquid crystal polyester. The content percentage of the liquid crystal polyester in relation to 100 mass% of the total content of the liquid crystal polyester and thermoplastic polyimide is 65 mass% or greater.
C08L 67/00 - Compositions of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Compositions of derivatives of such polymers
C08G 63/60 - Polyesters derived from hydroxy carboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from the reaction of a mixture of hydroxy carboxylic acids, polycarboxylic acids and polyhydroxy compounds
C08G 73/10 - Polyimides; Polyester-imides; Polyamide-imides; Polyamide acids or similar polyimide precursors
C08L 79/08 - Polyimides; Polyester-imides; Polyamide-imides; Polyamide acids or similar polyimide precursors
This electrolyte composition comprises: an ionically conductive inorganic solid electrolyte; a polymer having the ability to preferentially conduct metal ions; and an ionic liquid.
H01M 10/056 - Accumulators with non-aqueous electrolyte characterised by the materials used as electrolytes, e.g. mixed inorganic/organic electrolytes
H01B 1/06 - Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors mainly consisting of other non-metallic substances
H01B 1/08 - Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors mainly consisting of other non-metallic substances oxides
H01B 1/10 - Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors mainly consisting of other non-metallic substances sulfides
H01G 11/56 - Solid electrolytes, e.g. gels; Additives therein
H01M 10/056 - Accumulators with non-aqueous electrolyte characterised by the materials used as electrolytes, e.g. mixed inorganic/organic electrolytes
H01B 1/06 - Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors mainly consisting of other non-metallic substances
An electrolyte composition comprising an ion-conductive inorganic solid electrolyte, a polymer having the ability to preferentially conduct metal ions, and an organic solvent, the electrolyte composition satisfying that the content of the ion-conductive inorganic solid electrolyte is (1) 50 mass% or greater with respect to the whole electrolyte composition and/or (2) 15 vol% or greater with respect to the whole electrolyte composition.
H01M 10/056 - Accumulators with non-aqueous electrolyte characterised by the materials used as electrolytes, e.g. mixed inorganic/organic electrolytes
H01B 1/06 - Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors mainly consisting of other non-metallic substances
H01B 1/08 - Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors mainly consisting of other non-metallic substances oxides
H01B 1/10 - Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors mainly consisting of other non-metallic substances sulfides
H01G 11/56 - Solid electrolytes, e.g. gels; Additives therein
A touch sensor includes a sensing part in which a plurality of sensing cells is arranged and connected and a wiring part connected to the sensing part and formed outside the sensing part. The wiring part includes a first divisional wiring part having a plurality of first divisional wires having a connecting protrusion with a width larger than that of the wiring at one end thereof and a second divisional wiring part having a plurality of second divisional wires having one end thereof with a width smaller than that of the connecting protrusion and coupled to and overlapped with the connecting protrusion. The first divisional wiring part and the second divisional wiring part are formed by divisional exposure.
There is provided a piezoelectric stack including: a substrate (1); a bottom electrode film (2) on the substrate; a piezoelectric film (3) on the bottom electrode film, having a planar area smaller than a planar area of the bottom electrode film; a top electrode film (4) on the piezoelectric film; and an insulating film (5) provided from the top electrode film to the bottom electrode film and covering at least a part of a side surface of the piezoelectric film, wherein the insulating film has a slope (9a) filling a step between a top surface of the top electrode film and a top surface of the bottom electrode film, and the slope has a shape alleviating the step.
H10N 30/03 - Assembling devices that include piezoelectric or electrostrictive parts
H10N 30/00 - Piezoelectric or electrostrictive devices
H10N 30/063 - Forming interconnections, e.g. connection electrodes of multilayered piezoelectric or electrostrictive parts
H10N 30/076 - Forming of piezoelectric or electrostrictive parts or bodies on an electrical element or another base by depositing piezoelectric or electrostrictive layers, e.g. aerosol or screen printing by vapour phase deposition
H10N 30/077 - Forming of piezoelectric or electrostrictive parts or bodies on an electrical element or another base by depositing piezoelectric or electrostrictive layers, e.g. aerosol or screen printing by liquid phase deposition
H10N 30/87 - Electrodes or interconnections, e.g. leads or terminals
A herbicidal composition including ethyl [3-[2-chloro-4-fluoro-5-(1-methyl-6-trifluoromethyl-2,4-dioxo-1,2,3,4-tetrahydropyrimidin-3-yl)phenoxy]-2-pyridyloxylacetate and a herbicide selected from the group consisting of bicyclopyrone, mesotrione, tembotrione, isoxaflutole, pyrasulfotole, topramezone, and tolpyralate. A weight ratio of ethyl [3-[2-chloro-4-fluoro-5-(1-methyl-6-trifluoromethyl-2,4-dioxo-1,2,3,4-tetrahydropyrimidin-3-yl)phenoxy]-2-pyridyloxylacetate to the herbicide is from 1:1 to 1:42.
C07D 401/12 - Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
59.
ION CONDUCTIVE SUBSTANCE, ELECTROLYTE, AND BATTERY
An ion conductive substance comprising: an alkali metal element; a tetravalent metal element M; a halogen element; a dopant element X; and an oxygen element, wherein the content of the dopant element X is 50 mol% or less with respect to the content of the metal element M, and, in an X-ray diffraction chart obtained by measuring the ion conductive substance using a CuKα ray at 25°C, a diffraction peak having a half width of 2.0-10° exists in a range of 10-20° for the 2θ angle.
H01B 1/06 - Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors mainly consisting of other non-metallic substances
C01B 25/45 - Phosphates containing plural metal, or metal and ammonium
The purpose of the present invention is to provide a colorant capable of producing a coating film having enhanced green spectral characteristics. The colorant of the present invention contains a compound represented by formula (I) and is characterized in that the ratio of the number of groups represented by formula (T-2) to the number of Al atoms in the compound represented by formula (I) in the colorant is from 0.1 to 3. [In formula (I), R1and R2each independently represent a hydrogen atom, a hydroxy group, -R13, or -O-R13. When at least one of R1and R2represents -R13or -O-R13, R1and R2may bond to each other to form a ring. Ring T1, ring T2, ring T3, and ring T4 each independently represent a group represented by formula (T-1) or formula (T-2).]
Provided is an ingredient for a feed for aquatic animals, the ingredient serving as an ingredient in fish-meal substitute. This ingredient for a feed for aquatic animals contains secretions from insects of the infraorder Muscomorpha.
A method is provided for producing a resin composition including an olefin-based polymer; an inorganic filler; and a lubricant, in which the olefin-based polymer is at least one polymer selected from a propylene-based polymer and an ethylene-based polymer having a melt flow rate of 0.5 g/10 minutes or more measured at a temperature of 190° C. and a load of 2.16 kg. The method includes a step (1) of mixing the inorganic filler and a lubricant; a step (2) of mixing a mixture obtained in the step (1) and the olefin-based polymer; and a step (3) of kneading a mixture obtained in the step (2).
A propylene production method includes: a reaction step of supplying a fresh raw material and a recycled raw material to a reactor to obtain a crude product; a gas-liquid separation step of separating the crude product into a gas phase and a liquid phase; a propylene recovery step of recovering propylene from the gas phase; and a recycling step of recovering the recycled raw material from the liquid phase.
C07C 1/207 - Preparation of hydrocarbons from one or more compounds, none of them being a hydrocarbon starting from organic compounds containing only oxygen atoms as hetero atoms from carbonyl compounds
64.
ALKALI METAL ELEMENT-CONTAINING HALIDE, ELECTROLYTE, BATTERY, AND METHOD FOR PRODUCING HALIDE SOLID ELECTROLYTE
H01B 1/06 - Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors mainly consisting of other non-metallic substances
C01F 17/36 - Compounds containing rare earth metals and at least one element other than a rare earth metal, oxygen or hydrogen, e.g. La4S3Br6 halogen being the only anion, e.g. NaYF4
H01G 11/56 - Solid electrolytes, e.g. gels; Additives therein
maxmax to the long wavelength side in the absorption spectrum thereof. A compound according to the present invention is characterized by being represented by formula (I). [In formula (I), R1represents a C2-20 unsaturated aliphatic hydrocarbon group that may have a substituent, and R2represents a hydrogen atom, a C1-20 hydrocarbon group that may have a substituent, or a single bond that joins Z2and R1. Z1and Z2 independently represent a single bond or an oxygen atom.]
NATIONAL INSTITUTE OF ADVANCED INDUSTRIAL SCIENCE AND TECHNOLOGY (Japan)
AINO UNIVERSITY (Japan)
Inventor
Ozoe, Atsufumi
Kobayashi, Kentaro
Takahashi, Yasuhiko
Matsunaga, Kohei
Sato, Takaaki
Mizutani, Yoichi
Abstract
The present invention provides a technology for performing a test for prostate cancer. This method is for testing the possibility of having prostate cancer, the method comprising (1) measuring the amount or concentration of a biomarker in a body fluid sample collected from a subject, the biomarker being at least one member selected from the group consisting of dimethyl glutarate, 2,6-xylidine, 2-hydroxy-2-methylpropiophenone, 2,6-di(propan-2-yl) phenol, dimethyl succinate, acetophenone, 2-phenyl-2-propanol, and 3,5,5-trimetyl-2-cyclohexenone.
A material comprising an electron-accepting unit of formula (I): Ar is an aromatic ring; Ar1 is a substituted or unsubstituted 5- or 6-membered heteroaromatic ring containing N and C ring atoms; when Ar1 is a substituted or unsubstituted 6-membered heteroaromatic ring, Ar2 is a substituted or unsubstituted 6-membered heteroaromatic ring wherein the ring atoms are selected from N and C; when Ar1 is a 5-membered heteroaromatic ring, Ar2 is a substituted or unsubstituted 5- or 6-membered heteroaromatic ring; Ar3 is a 5-membered ring or a substituted or unsubstituted 6-membered ring; Ar4 is a 5-membered ring or a substituted or unsubstituted 6-membered ring or is absent; Ar5 is a substituted or unsubstituted monocyclic or polycyclic group containing at least one aromatic or heteroaromatic ring; Ar6 is a substituted or unsubstituted monocyclic or polycyclic group containing at least one aromatic or heteroaromatic ring or is absent; and each X is independently a substituent bound to a C atom of Ar3, and where present Ar4, with the proviso that at least one X is an electron withdrawing group; and wherein the material further comprises an electron-donating unit.
A material comprising an electron-accepting unit of formula (I): Ar is an aromatic ring; Ar1 is a substituted or unsubstituted 5- or 6-membered heteroaromatic ring containing N and C ring atoms; when Ar1 is a substituted or unsubstituted 6-membered heteroaromatic ring, Ar2 is a substituted or unsubstituted 6-membered heteroaromatic ring wherein the ring atoms are selected from N and C; when Ar1 is a 5-membered heteroaromatic ring, Ar2 is a substituted or unsubstituted 5- or 6-membered heteroaromatic ring; Ar3 is a 5-membered ring or a substituted or unsubstituted 6-membered ring; Ar4 is a 5-membered ring or a substituted or unsubstituted 6-membered ring or is absent; Ar5 is a substituted or unsubstituted monocyclic or polycyclic group containing at least one aromatic or heteroaromatic ring; Ar6 is a substituted or unsubstituted monocyclic or polycyclic group containing at least one aromatic or heteroaromatic ring or is absent; and each X is independently a substituent bound to a C atom of Ar3, and where present Ar4, with the proviso that at least one X is an electron withdrawing group; and wherein the material further comprises an electron-donating unit.
C07D 519/00 - Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups or
H10K 71/15 - Deposition of organic active material using liquid deposition, e.g. spin coating characterised by the solvent used
The present invention addresses the problem of realizing a high recovery rate even when the raw material supply rate is particularly high. The present invention pertains to a regenerated methyl(meth)acrylate production method comprising: a thermal decomposition step for thermally decomposing a methyl(meth)acrylate-based polymer composition that contains one or more methyl(meth)acrylate-based polymers and includes a methyl(meth)acrylate-based polymer having a viscosity average molecular weight of 800000-5000000; and a recovery step for recovering a regenerated methyl(meth)acrylate generated in the thermal decomposition step.
C07C 67/475 - Preparation of carboxylic acid esters by splitting of carbon-to-carbon bonds and redistribution, e.g. disproportionation or migration of groups between different molecules
C08J 11/12 - Recovery or working-up of waste materials of polymers by chemically breaking down the molecular chains of polymers or breaking of crosslinks, e.g. devulcanisation by dry-heat treatment only
69.
POSITIVE ELECTRODE ACTIVE MATERIAL FOR LITHIUM SECONDARY BATTERY, ELECTRODE FOR LITHIUM SECONDARY BATTERY, AND LITHIUM SECONDARY BATTERY
This positive electrode active material for a lithium secondary battery has a layered structure that includes secondary particles that are an aggregate of primary particles, and includes an element M1 and an element M2, wherein the element M1 is at least one element selected from the group consisting of Nb, W, Mo, Ta, La, B, and P, the element M2 is at least one element M2 selected from the group consisting of Ni, Co, and Mn, and formulas (1) and (2) are satisfied.
H01M 4/525 - Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of nickel, cobalt or iron of mixed oxides or hydroxides containing iron, cobalt or nickel for inserting or intercalating light metals, e.g. LiNiO2, LiCoO2 or LiCoOxFy
H01M 4/36 - Selection of substances as active materials, active masses, active liquids
H01M 4/505 - Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of manganese of mixed oxides or hydroxides containing manganese for inserting or intercalating light metals, e.g. LiMn2O4 or LiMn2OxFy
A polymer comprising a repeating structure of formula (I) wherein Ar in each occurrence is an arylene or heteroarylene group; p is at least 2; one of Y1 and Y2 is CR1 wherein R1 is H or a substituent; and the other of Y1 and Y2 is N. The polymer may be formed by reaction of monomers containing reactive groups which react to form an imine. The polymer may be used as a thermally conductive polymer, e.g. a thermally conductive layer of an electronic device.
A polymer comprising a repeating structure of formula (I) wherein Ar in each occurrence is an arylene or heteroarylene group; p is at least 2; one of Y1 and Y2 is CR1 wherein R1 is H or a substituent; and the other of Y1 and Y2 is N. The polymer may be formed by reaction of monomers containing reactive groups which react to form an imine. The polymer may be used as a thermally conductive polymer, e.g. a thermally conductive layer of an electronic device.
A process or apparatus for producing polyethylene with improved film thinning and handleability involves polymerizing high-pressure ethylene using an autoclave-type reactor in the presence of a polymerization initiator. The reaction zone of the reactor has at least two different temperature sections; the polymerization initiator and the ethylene are supplied to the upstream temperature section in the reaction zone and the ethylene is polymerized to generate polyethylene; unreacted ethylene and the polyethylene generated at the upstream temperature section in the reactor flow into the downstream temperature section in communication with the upstream temperature section, so that additional polyethylene is generated at the downstream temperature section. A difference (ΔT [° C.]) between a temperature (T1 [° C.]) of the temperature section positioned upstream and a temperature (T2 [° C.]) of the temperature section positioned downstream in the reaction zone that receives the polymerization initiator and is in the autoclave-type reactor is 2.1° C. to 8.4° C.
This method for producing a positive electrode active material comprises the following steps. (1) a step in which an activation agent containing at least one compound that is selected from the group consisting of a potassium compound and a sodium compound is mixed into an electrode mixture which contains a positive electrode active material, a binder and an electrolyte, and from which at least some of the electrolyte is removed by means of a contact with an electrolyte cleaning solvent (2) a step in which the thus-obtained mixture is heated to a retention temperature that is not less than the melting initiation temperature of the activation agent, so that the positive electrode active material contained in the mixture is activated (3) a step in which the mixture after heating is brought into contact with a liquid that contains water, thereby obtaining a slurry that contains a solid component and a liquid component, and subsequently, the slurry is separated into the solid component and the liquid component, wherein the total content of potassium and sodium in the liquid component after the separation is 0.090 to 2.0% by mass, and the total content of potassium and sodium in the solid component after the separation is 1.2% by mass or less
H01M 10/54 - Reclaiming serviceable parts of waste accumulators
C22B 7/00 - Working-up raw materials other than ores, e.g. scrap, to produce non-ferrous metals or compounds thereof
H01M 4/505 - Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of manganese of mixed oxides or hydroxides containing manganese for inserting or intercalating light metals, e.g. LiMn2O4 or LiMn2OxFy
H01M 4/525 - Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of nickel, cobalt or iron of mixed oxides or hydroxides containing iron, cobalt or nickel for inserting or intercalating light metals, e.g. LiNiO2, LiCoO2 or LiCoOxFy
This positive electrode active material for a lithium secondary battery contains a composite oxide containing at least one element selected from the following element group 1, and at least one element selected from the following element group 2, and satisfies requirements (1)-(3). Element group 1: Ni, Co, Mn, Fe, Al, and P. Element group 2: Li, Na, K, Ca, Sr, Ba, and Mg. Requirement (1): The active material contains fluorine, sulfur, and potassium, and the total amount of fluorine, sulfur, and potassium is 0.12-10.0 mass%. Requirement (2): When the concentration of potassium in the active material is defined as CK (mass%) and the concentration of sulfur in the active material is defined as CS (mass%), CK/CS is 0.0001-2.0. Requirement (3): When the concentration of fluorine in the active material is defined as CF (mass%) and the concentration of sulfur in the active material is defined as CS (mass%), CF/CS is 0.0001-20.0.
H01M 4/525 - Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of nickel, cobalt or iron of mixed oxides or hydroxides containing iron, cobalt or nickel for inserting or intercalating light metals, e.g. LiNiO2, LiCoO2 or LiCoOxFy
H01M 4/505 - Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of manganese of mixed oxides or hydroxides containing manganese for inserting or intercalating light metals, e.g. LiMn2O4 or LiMn2OxFy
H01M 10/54 - Reclaiming serviceable parts of waste accumulators
The present invention addresses the problem of providing a new compound having excellent film formability and curability that can yield a cured product that exhibits a high refractive index. The present invention relates to a compound that is represented by formula (I). In the formula, L represents a divalent group; multiple L may be the same or different. m represents 0 or 1; multiple m may be the same or different. A represents an O atom or an S atom; multiple A may be the same or different. n represents any integer of 0 to 3; multiple n may be the same or different. R represents a monovalent substituent; when there are multiple R, the multiple R may be the same or different. R2represents a hydrogen atom or a monovalent substituent; multiple R2 may be the same or different. Two groups having S atoms bond to positions 1 and 6, positions 2 and 6, or positions 2 and 7 of the naphthalene ring.
C08G 59/02 - Polycondensates containing more than one epoxy group per molecule
C08G 59/14 - Polycondensates modified by chemical after-treatment
C08G 59/30 - Di-epoxy compounds containing atoms other than carbon, hydrogen, oxygen, and nitrogen
C08G 75/06 - Polythioethers from cyclic thioethers
C08G 75/08 - Polythioethers from cyclic thioethers from thiiranes
G02B 1/04 - Optical elements characterised by the material of which they are made; Optical coatings for optical elements made of organic materials, e.g. plastics
G09F 9/30 - Indicating arrangements for variable information in which the information is built-up on a support by selection or combination of individual elements in which the desired character or characters are formed by combining individual elements
H01L 21/301 - Treatment of semiconductor bodies using processes or apparatus not provided for in groups to subdivide a semiconductor body into separate parts, e.g. making partitions
75.
COMPOSITION, CURED PRODUCT, DISPLAY DEVICE, AND SOLID-STATE IMAGING ELEMENT
The present invention provides a novel composition that has superior curability and can provide a cured product demonstrating a high refractive index. The present invention relates to a composition including a compound represented by formula (I), and an alkali-soluble resin. In formula (I), n represents an integer from 0 to 6, L represents a single bond or a divalent group, the plurality of Ls may be the same or different, R11represents a monovalent substituent, if there are a plurality of R11s then the plurality of R11s may be the same or different, R12is selected from the group consisting of a hydrogen atom, formula (1a), and formula (1b), and the plurality of R12s may be the same or different.
C08G 75/06 - Polythioethers from cyclic thioethers
C08L 101/12 - Compositions of unspecified macromolecular compounds characterised by physical features, e.g. anisotropy, viscosity or electrical conductivity
G09F 9/30 - Indicating arrangements for variable information in which the information is built-up on a support by selection or combination of individual elements in which the desired character or characters are formed by combining individual elements
76.
SOLID CATALYST COMPONENT FOR OLEFIN POLYMERIZATION
To produce an olefin-based polymer having a minor amount of decrease in bulk density due to heat.
To produce an olefin-based polymer having a minor amount of decrease in bulk density due to heat.
A solid catalyst component for olefin polymerization containing a titanium atom, a magnesium atom, a halogen atom, and an internal electron donor, and having an envelope E1 calculated by the following Formula (1) in a range of 0.810 to 0.920.
To produce an olefin-based polymer having a minor amount of decrease in bulk density due to heat.
A solid catalyst component for olefin polymerization containing a titanium atom, a magnesium atom, a halogen atom, and an internal electron donor, and having an envelope E1 calculated by the following Formula (1) in a range of 0.810 to 0.920.
E1=LE1/LS1 (1)
To produce an olefin-based polymer having a minor amount of decrease in bulk density due to heat.
A solid catalyst component for olefin polymerization containing a titanium atom, a magnesium atom, a halogen atom, and an internal electron donor, and having an envelope E1 calculated by the following Formula (1) in a range of 0.810 to 0.920.
E1=LE1/LS1 (1)
(In Formula, LE1 is a convex hull perimeter of the solid catalyst component for olefin polymerization obtained from an image of the solid catalyst component for olefin polymerization captured with a scanning electron microscope, and LS1 is an actual perimeter of the solid catalyst component for olefin polymerization obtained from the image of the solid catalyst component for olefin polymerization captured with the scanning electron microscope.)
C08F 4/16 - Metallic compounds other than hydrides and other than metallo-organic compounds; Boron halide or aluminium halide complexes with organic compounds containing oxygen of silicon, germanium, tin, lead, titanium, zirconium or hafnium
C08F 4/12 - Metallic compounds other than hydrides and other than metallo-organic compounds; Boron halide or aluminium halide complexes with organic compounds containing oxygen of boron, aluminium, gallium, indium, thallium, or rare earths
77.
PHOTOELECTRIC CONVERSION ELEMENT, INK FOR PRODUCING PHOTOELECTRIC CONVERSION ELEMENT, METHOD FOR MANUFACTURING PHOTOELECTRIC CONVERSION ELEMENT, IMAGE SENSOR, AND FINGERPRINT AUTHENTICATION DEVICE
The present invention addresses the problem of providing a photoelectric conversion element in which an increase in dark current after heat treatment is suppressed. The present invention relates to a photoelectric conversion element having: an anode (12); a cathode (16); an active layer (14) provided between the anode (12) and the cathode (16); and intermediate layers (13, 15) provided between the anode (12) and the active layer (14) and/or between the cathode (16) and the active layer (14). The intermediate layers (13, 15) contain a non-ionic insulating polymer.
H10K 30/60 - Organic devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation in which radiation controls flow of current through the devices, e.g. photoresistors
H10K 30/30 - Organic devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation comprising bulk heterojunctions, e.g. interpenetrating networks of donor and acceptor material domains
H10K 30/82 - Transparent electrodes, e.g. indium tin oxide [ITO] electrodes
A sputtering target material made of a sintered object of an oxide comprising potassium, sodium, niobium, and oxygen, the sputtering target material having a density of 4.2 g/cm3 or less and a Vickers hardness of 30-200, wherein a plurality of crystal grains observed in the sputter surface have an area-average grain diameter of 3.0 μm or larger.
C04B 35/495 - Shaped ceramic products characterised by their composition; Ceramic compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxides based on vanadium, niobium, tantalum, molybdenum or tungsten oxides or solid solutions thereof with other oxides, e.g. vanadates, niobates, tantalates, molybdates or tungstates
H10N 30/076 - Forming of piezoelectric or electrostrictive parts or bodies on an electrical element or another base by depositing piezoelectric or electrostrictive layers, e.g. aerosol or screen printing by vapour phase deposition
H10N 30/097 - Forming inorganic materials by sintering
This positive electrode active material for lithium secondary batteries comprises a plurality of secondary particles, in each of which a plurality of primary particles aggregate; and this positive electrode active material for lithium secondary batteries satisfies the requirements described below. (1) The secondary particles each internally comprise a plurality of voids, and the value at a cumulative frequency of 50% in the area-based cumulative frequency distribution of the circle-equivalent diameters of the voids on the basis of the cross-sectional images of the secondary particles is more than 0.2 µm but not more than 0.65 µm, while the value at a cumulative frequency of 50% in the area-based cumulative frequency distribution of the circularity of the voids on the basis of the cross-sectional images of the secondary particles is 2.2 to 6.5. (2) The primary particles are formed of an oxide which contains one or more elements that are selected from the element group 1 shown below and one or more elements that are selected from the element group 2 shown below. Element group 1: Ni, Co, Mn, Fe, Al and P Element group 2: Li, Na, K, Ca, Sr, Ba and Mg
H01M 4/525 - Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of nickel, cobalt or iron of mixed oxides or hydroxides containing iron, cobalt or nickel for inserting or intercalating light metals, e.g. LiNiO2, LiCoO2 or LiCoOxFy
H01M 4/505 - Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of manganese of mixed oxides or hydroxides containing manganese for inserting or intercalating light metals, e.g. LiMn2O4 or LiMn2OxFy
H01M 10/54 - Reclaiming serviceable parts of waste accumulators
80.
PRODUCTION METHOD FOR POSITIVE ELECTRODE ACTIVE MATERIAL
This production method for a positive electrode active material comprises the following steps. (1) A step for bringing an electrode mixture containing a positive electrode active material, a binder member, and an electrolyte into contact with an electrolyte cleaning solvent to obtain a slurry including solid components and liquid components, and thereafter, separating the slurry into the solid components and the liquid components, wherein, in the liquid components after the separation, the P amount is 0.0020-2.0 mass% and the F amount is 0.01-7.0 mass%, and, in the solid components after the separation, the P amount remaining therein is 0.7 mass% or less. (2) A step for mixing an activation agent containing one or more alkali metal compounds with the separated solid components. (3) A step for heating the obtained mixture to a retention temperature not less than the melting start temperature of the activation agent so as to activate the positive electrode active material contained in the mixture.
H01M 10/54 - Reclaiming serviceable parts of waste accumulators
C22B 7/00 - Working-up raw materials other than ores, e.g. scrap, to produce non-ferrous metals or compounds thereof
H01M 4/505 - Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of manganese of mixed oxides or hydroxides containing manganese for inserting or intercalating light metals, e.g. LiMn2O4 or LiMn2OxFy
H01M 4/525 - Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of nickel, cobalt or iron of mixed oxides or hydroxides containing iron, cobalt or nickel for inserting or intercalating light metals, e.g. LiNiO2, LiCoO2 or LiCoOxFy
81.
METHOD FOR PRODUCING POSITIVE ELECTRODE ACTIVE MATERIAL
This method for producing a positive electrode active material comprises the steps described below. (1) A mixture is obtained by mixing an activation agent which contains one or more alkali metal compounds into an electrode mixture which contains a positive electrode active material, a binder and an electrolyte, and from which at least some of the electrolyte is removed by means of a contact with an electrolyte cleaning solvent. (2) The mixture is heated to a retention temperature that is not less than the melting initiation temperature of the activation agent. (3) The mixture after the step (2) is brought into contact with a liquid that contains water, thereby obtaining a slurry that contains a solid component and a liquid component, and subsequently, the slurry is separated into the solid component and the liquid component. (4) The thus-obtained solid component is exposed to heat and/or a reduced pressure environment, thereby removing water from the solid component, and within 24 hours from the separation of the slurry into the solid component and the liquid component, the ambient pressure at which the solid component is present and/or the temperature of the solid component is changed so that the ratio of the saturated water vapor pressure at the temperature of the solid component to the ambient pressure is 80% or more. (5) The solid component after the step (4) is subjected to a heat treatment at less than 900°C.
H01M 10/54 - Reclaiming serviceable parts of waste accumulators
C22B 7/00 - Working-up raw materials other than ores, e.g. scrap, to produce non-ferrous metals or compounds thereof
H01M 4/505 - Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of manganese of mixed oxides or hydroxides containing manganese for inserting or intercalating light metals, e.g. LiMn2O4 or LiMn2OxFy
H01M 4/525 - Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of nickel, cobalt or iron of mixed oxides or hydroxides containing iron, cobalt or nickel for inserting or intercalating light metals, e.g. LiNiO2, LiCoO2 or LiCoOxFy
The present invention addresses the problem of providing a novel compound which enables the production of a cured article having a high refraction index and which has excellent moldability and curability. The present invention relates to a compound that is represented by formula (I). In the formula, a plurality of L's each independently represents a bivalent group and may be the same as or different from each other; a plurality of m's each independently represent 0 or 1 and may be the same as or different from each other; n represents an integer of 0 to 6; R represents a monovalent substituent, and when there are a plurality of R's, the R's may be the same as or different from each other; and a plurality of R2's each represents a hydrogen atom or a monovalent substituent, and the R2's may be the same as or different from each other.
C08G 75/06 - Polythioethers from cyclic thioethers
C08G 75/08 - Polythioethers from cyclic thioethers from thiiranes
G02B 1/04 - Optical elements characterised by the material of which they are made; Optical coatings for optical elements made of organic materials, e.g. plastics
G09F 9/30 - Indicating arrangements for variable information in which the information is built-up on a support by selection or combination of individual elements in which the desired character or characters are formed by combining individual elements
H01L 21/301 - Treatment of semiconductor bodies using processes or apparatus not provided for in groups to subdivide a semiconductor body into separate parts, e.g. making partitions
83.
COMPOSITION, CURED PRODUCT, DISPLAY DEVICE, AND SOLID-STATE IMAGING DEVICE
The present invention provides a novel composition that can yield a cured product having a high refractive index and has excellent curability. The present invention pertains to a composition comprising: a compound represented by formula (I); and a resin having a refractive index of at least 1.60 at a wavelength of 550 nm. In formula (I), n represents an integer of 0-6, L represents a single bond or a divalent group, a plurality of L's may be the same or different, R11represents a monovalent substituent (when there is a plurality of R11's, the plurality of R11may be the same or different), R12is selected from the group consisting of a hydrogen atom, formula (1a), and formula (1b), and a plurality of R12's may be the same or different.
C08G 75/06 - Polythioethers from cyclic thioethers
C08L 101/12 - Compositions of unspecified macromolecular compounds characterised by physical features, e.g. anisotropy, viscosity or electrical conductivity
G09F 9/30 - Indicating arrangements for variable information in which the information is built-up on a support by selection or combination of individual elements in which the desired character or characters are formed by combining individual elements
The present invention addresses the problem of providing a novel compound that is capable of providing a cured product exhibiting a high refractive index, and has excellent curability. The present invention relates to a compound that is represented by formula (I). In the formula and in the compound represented by formula (I), R represents a monovalent hydrocarbon group, and if there are a plurality of Rs, the plurality of Rs may be may be the same or different. The symbol n represents an average value that is a number of 1 or greater. A represents an O atom or an S atom. The plurality of As may be the same or different, but at least one A is an S atom.
01 - Chemical and biological materials for industrial, scientific and agricultural use
17 - Rubber and plastic; packing and insulating materials
Goods & Services
Industrial chemicals; adhesives and glues for industrial
purposes; plastics (raw materials); synthetic resins,
unprocessed; artificial resins, unprocessed; plastics,
unprocessed. Synthetic resins, semi-processed; artificial resins,
semi-processed; plastic film, other than for wrapping;
semi-finished plastic products; plastic semi-worked products
in the form of pellets, rods, bars, foils, foams, fibers,
films, boards, plates, profiles, hoses, tubes, tapes,
strips, blocks and sheets; plastic substances,
semi-processed; plastic sheet materials for use in
manufacture; plastic fibers, other than for textile use;
chemical fiber, not for textile use; gum, raw or
semi-worked; rubber, raw or semi-worked; synthetic rubber;
natural rubber; insulating materials; insulators; electrical
insulators; electrical insulating materials; insulating
varnish; soundproofing materials of rock wool, not for
building purposes; asbestos powder; asbestos boards.
01 - Chemical and biological materials for industrial, scientific and agricultural use
17 - Rubber and plastic; packing and insulating materials
Goods & Services
Industrial chemicals; adhesives and glues for industrial
purposes; plastics (raw materials); synthetic resins,
unprocessed; artificial resins, unprocessed; plastics,
unprocessed. Synthetic resins, semi-processed; artificial resins,
semi-processed; plastic film, other than for wrapping;
semi-finished plastic products; plastic semi-worked products
in the form of pellets, rods, bars, foils, foams, fibers,
films, boards, plates, profiles, hoses, tubes, tapes,
strips, blocks and sheets; plastic substances,
semi-processed; plastic sheet materials for use in
manufacture; plastic fibers, other than for textile use;
chemical fiber, not for textile use; gum, raw or
semi-worked; rubber, raw or semi-worked; synthetic rubber;
natural rubber; insulating materials; insulators; electrical
insulators; electrical insulating materials; insulating
varnish; soundproofing materials of rock wool, not for
building purposes; asbestos powder; asbestos boards.
01 - Chemical and biological materials for industrial, scientific and agricultural use
17 - Rubber and plastic; packing and insulating materials
Goods & Services
Industrial chemicals; adhesives and glues for industrial
purposes; plastics (raw materials); synthetic resins,
unprocessed; artificial resins, unprocessed; plastics,
unprocessed. Synthetic resins, semi-processed; artificial resins,
semi-processed; plastic film, other than for wrapping;
semi-finished plastic products; plastic semi-worked products
in the form of pellets, rods, bars, foils, foams, fibers,
films, boards, plates, profiles, hoses, tubes, tapes,
strips, blocks and sheets; plastic substances,
semi-processed; plastic sheet materials for use in
manufacture; plastic fibers, other than for textile use;
chemical fiber, not for textile use; gum, raw or
semi-worked; rubber, raw or semi-worked; synthetic rubber;
natural rubber; insulating materials; insulators; electrical
insulators; electrical insulating materials; insulating
varnish; soundproofing materials of rock wool, not for
building purposes; asbestos powder; asbestos boards.
01 - Chemical and biological materials for industrial, scientific and agricultural use
17 - Rubber and plastic; packing and insulating materials
Goods & Services
Industrial chemicals; adhesives and glues for industrial
purposes; plastics (raw materials); synthetic resins,
unprocessed; artificial resins, unprocessed; plastics,
unprocessed. Synthetic resins, semi-processed; artificial resins,
semi-processed; plastic film, other than for wrapping;
semi-finished plastic products; plastic semi-worked products
in the form of pellets, rods, bars, foils, foams, fibers,
films, boards, plates, profiles, hoses, tubes, tapes,
strips, blocks and sheets; plastic substances,
semi-processed; plastic sheet materials for use in
manufacture; plastic fibers, other than for textile use;
chemical fiber, not for textile use; gum, raw or
semi-worked; rubber, raw or semi-worked; synthetic rubber;
natural rubber; insulating materials; insulators; electrical
insulators; electrical insulating materials; insulating
varnish; soundproofing materials of rock wool, not for
building purposes; asbestos powder; asbestos boards.
Provided is a compound represented by formula (1). In formula (1), Ar11, Ar12, and Ar13represent a 1,4-phenylene group, a 1,4-naphthylene group, or a divalent aromatic condensed heterocyclic group having two five-membered rings, and at least one of Ar11, Ar12, and Ar13represents a divalent aromatic condensed heterocyclic group. k represents 1 or 2. R11, R12, R13, and R14represent a hydrogen atom, a linear or cyclic aliphatic group, or an aryl group. At least one set of: R11and R12; and R13and R14may be connected to each other to form a ring in which at least one of the methylene units constituting the ring may be substituted with an oxygen atom or a carbonyl group. At least one of R11, R12, R13, and R14 may be substituted with at least one of an organosilyloxy group or a polymerizable group.
A compound represented by formula (1). [In formula (1): Ar is an arylene group; R1is a monovalent group represented by formula (2); and R2is a monovalent group represented by formula (3). In formula (2): R3is a hydrogen atom or an optionally branched alkyl group; m is an integer of 1 or greater; and * represents a bonding site to Ar. In formula (3): R4 is a hydrogen atom or an optionally branched alkyl group; n is an integer of 1 or greater; and * represents a bonding site to Ar.]
C07C 323/64 - Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and sulfur atoms, not being part of thio groups, bound to the same carbon skeleton
01 - Chemical and biological materials for industrial, scientific and agricultural use
17 - Rubber and plastic; packing and insulating materials
Goods & Services
Industrial chemicals; adhesives and glues for industrial
purposes; plastics (raw materials); synthetic resins,
unprocessed; artificial resins, unprocessed; plastics,
unprocessed. Synthetic resins, semi-processed; artificial resins,
semi-processed; plastic film, other than for wrapping;
semi-finished plastic products; plastic semi-worked products
in the form of pellets, rods, bars, foils, foams, fibers,
films, boards, plates, profiles, hoses, tubes, tapes,
strips, blocks and sheets; plastic substances,
semi-processed; plastic sheet materials for use in
manufacture; plastic fibers, other than for textile use;
chemical fiber, not for textile use; gum, raw or
semi-worked; rubber, raw or semi-worked; synthetic rubber;
natural rubber; insulating materials; insulators; electrical
insulators; electrical insulating materials; insulating
varnish; soundproofing materials of rock wool, not for
building purposes; asbestos powder; asbestos boards.
A resin composition including a liquid crystalline polymer and a fluororesin, wherein the fluororesin has a peak area percentage of a CF3 groups content relative to a CF2 groups content in the fluororesin of 0.05% or more, as determined by the following [Method for measuring CF3 groups content]: the CF3 groups content relative to the CF2 groups content in the fluororesin is calculated as an area percentage from a peak area ICF3 corresponding to the CF3 groups and a peak area ICF2 corresponding to the CF2 groups measured by 19F solid-state NMR, and is determined by the following formula (f1): CF3 groups content (%)={(ICF3/3)/(ICF2/2)}×100 (f1).
[Problem] To provide a laminate able to inhibit a color change when white is displayed (color emitted) being strongly felt, even when exposed to the outdoors for a long time. [Solution] This laminate has, in order, a first ultraviolet absorption layer, a first light-absorption anisotropic layer, a second ultraviolet absorption layer, and a second light-absorption anisotropic layer. The first light-absorption anisotropic layer is formed from a composition containing at least one dichroic dye and a liquid crystal compound. The second light-absorption anisotropic layer has an absorption axis in a horizontal direction with respect to a plane of the layer. The first ultraviolet absorption layer and the second ultraviolet absorption layer both satisfy the relationship given in formula (1). The first light-absorption anisotropic layer satisfies the relationship given in formula (2). (1) T(380)≤20; (2) Az>(Ax+Ay)/2; [In formula (1), T(380) represents the transmittance [%] at a wavelength of 380 nm. In formula (2), Ax, Ay, and Az represent an absorbance of linearly polarized light oscillating in the x-axis direction, the y-axis direction, and the z-axis direction, respectively, said absorbance being of a maximum wavelength of absorption of the first light-absorption anisotropic layer in the range of wavelengths of 410-780 nm, inclusive. The x axis is a direction that is parallel to the absorption axis direction of the second light-absorption anisotropic layer in a plane of the first light-absorption anisotropic layer. The y axis is a direction that is orthogonal to the x axis in the plane of the first light-absorption anisotropic layer. The z axis is a direction that is orthogonal to the x axis and the y axis.]
G09F 9/00 - Indicating arrangements for variable information in which the information is built-up on a support by selection or combination of individual elements
G09F 9/30 - Indicating arrangements for variable information in which the information is built-up on a support by selection or combination of individual elements in which the desired character or characters are formed by combining individual elements
Provided is a mixed composition for a polymerizable liquid crystal compound that has a low phase transition temperature and is preferably suited to production of a retardation film that has excellent optical characteristics.
C08F 220/30 - Esters containing oxygen in addition to the carboxy oxygen containing aromatic rings in the alcohol moiety
C07D 277/66 - Benzothiazoles with only hydrocarbon or substituted hydrocarbon radicals attached in position 2 with aromatic rings or ring systems directly attached in position 2
Provided is a layered body comprising a metal particle aggregate layer, which is formed from multiple metal particles disposed spaced apart from each other, and a silicon-atom-containing layer. The silicon-atom-containing layer has a first surface. The signal strength of carbon atoms in the first surface is 20.0 at% or less as determined by X-ray photoelectron spectroscopy.
B32B 15/04 - Layered products essentially comprising metal comprising metal as the main or only constituent of a layer, next to another layer of a specific substance
G01N 23/2273 - Measuring photoelectron spectra, e.g. electron spectroscopy for chemical analysis [ESCA] or X-ray photoelectron spectroscopy [XPS]
Provided is a hydrophilic oil repellent polymer having excellent shape transferability during molding that exhibits a high antifouling property in humid environments due to having high oil repellency in water. The polymer comprises: a structural unit A derived from ethylene and/or propylene; a structural unit B of formula (1); and a structural unit C of formula (2). In formula (1), L162nn-(Rf2pp-(Rf3hh-(Si(Rf42gg-Si(Rf133, Rf11-151-15 alkyl group, Rf2and Rf31-151-15 alkylene group, Rf41-156-206-20 aryl group, n represents an integer of 0-10, p represents an integer of 0-15, h represents an integer of 0-15, and g represents an integer of 1-1000. In formula (2), L262mm-(Rr2qq-Rr1, Rr11-151-201-20 aryl group, Rr21-151-15 alkylene group, q represents an integer of 1-1,000,000, and m represents an integer of 0-10.
C08G 81/02 - Macromolecular compounds obtained by interreacting polymers in the absence of monomers, e.g. block polymers at least one of the polymers being obtained by reactions involving only carbon-to-carbon unsaturated bonds
C08F 8/42 - Introducing metal atoms or metal-containing groups
C08F 210/00 - Copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
C08L 87/00 - Compositions of unspecified macromolecular compounds, obtained otherwise than by polymerisation reactions only involving unsaturated carbon-to-carbon bonds
C08L 101/00 - Compositions of unspecified macromolecular compounds
C09D 187/00 - Coating compositions based on unspecified macromolecular compounds, obtained otherwise than by polymerisation reactions only involving unsaturated carbon-to-carbon bonds
98.
POLYMER, RESIN COMPOSITION, MOLDED BODY, AND POLYMER PRODUCTION METHOD
Provided is a polymer that exhibits water repellency and oil repellency, has excellent functionality in suppressing the adhesion of slime, and exhibits excellent shape transferability when molded. Also provided are a resin composition, a molded body, and a method for producing said polymer. The polymer comprises: a constituent unit (A) derived from ethylene and/or propylene; a constituent unit (B) from formula (1) below; and a constituent unit (C) from formula (2) below. In formula (1), L62nn-(Rf2pp-(Rf3hh-(Si(Rf42gg-Si(Rf133, Rf11-151-15 alkyl group, Rf2and Rf31-151-15 alkylene group, Rf41-156-206-20 aryl group, n is an integer from 0-10, p is an integer from 0-15, h is an integer from 0-15, and g is an integer from 1-1000. In formula (2), L522OH, a carboxy group, a hydroxyl group, an amino group, or an alkyl amino group having 1-4 carbon atoms.
C08G 81/02 - Macromolecular compounds obtained by interreacting polymers in the absence of monomers, e.g. block polymers at least one of the polymers being obtained by reactions involving only carbon-to-carbon unsaturated bonds
C08F 8/42 - Introducing metal atoms or metal-containing groups
C08F 210/00 - Copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
C08L 87/00 - Compositions of unspecified macromolecular compounds, obtained otherwise than by polymerisation reactions only involving unsaturated carbon-to-carbon bonds
C08L 101/00 - Compositions of unspecified macromolecular compounds
C09D 187/00 - Coating compositions based on unspecified macromolecular compounds, obtained otherwise than by polymerisation reactions only involving unsaturated carbon-to-carbon bonds
05 - Pharmaceutical, veterinary and sanitary products
10 - Medical apparatus and instruments
42 - Scientific, technological and industrial services, research and design
44 - Medical, veterinary, hygienic and cosmetic services; agriculture, horticulture and forestry services
Goods & Services
Pharmaceutical preparations for use in cancer testing; diagnostic kits consisting primarily of reagents for use in cancer testing Medical apparatus for detecting cancer Testing, inspection or research of pharmaceuticals, cosmetics or foodstuffs; medical research services in the field of cancer; medical and scientific research in the field of cancer treatment and diagnosis; medical research services; development of pharmaceutical preparations and medicines; design, maintenance, development and updating of computer software Medical analysis services for the diagnosis of cancer; medical diagnosis of cancer; providing cancer screening services; providing information in the field of cancer prevention, screening, diagnosis and treatment; providing medical information; rental of medical apparatus for detecting cancer; rental of medical apparatus and instruments
100.
LITHIUM METAL COMPOSITE OXIDE, POSITIVE ELECTRODE ACTIVE MATERIAL FOR LITHIUM SECONDARY BATTERY, POSITIVE ELECTRODE FOR LITHIUM SECONDARY BATTERY, AND LITHIUM SECONDARY BATTERY
An object of the present invention is to provide a lithium metal composite oxide, when used as a positive electrode active material for a lithium secondary battery, capable of obtaining a lithium secondary battery having a high cycle retention rate, and a positive electrode active material for a lithium secondary battery, a positive electrode for a lithium secondary battery, and a lithium secondary battery in which the lithium metal composite oxide is used. This lithium metal composite oxide is a particulate lithium metal composite oxide, comprising first particles having a particle diameter equal to or less than a 50% cumulative volume particle size D50 of the lithium metal composite oxide and second particles having a particle diameter exceeding the D50, in which the D50 is 2 to 20 μm, an average particle strength PS of the first particles is larger than an average particle strength PB of the second particles, and a standard deviation σS of the particle strength of the first particles is larger than a standard deviation σB of the particle strength of the second particles.
H01M 4/525 - Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of nickel, cobalt or iron of mixed oxides or hydroxides containing iron, cobalt or nickel for inserting or intercalating light metals, e.g. LiNiO2, LiCoO2 or LiCoOxFy
